Medical Devices Regulation and In Vitro Regulation: Council First-Reading Position, Next Steps and Implementation

As you may be aware, on 7 March, the Council adopted its much expected First-Reading Position on both the Medical Devices Regulations (MDR) and in vitro diagnostics Regulation (IVDR), bringing the MD and diagnostic community one step closer to the entry into force of the two Regulations.

Shortly after, on 9 March, the EU Commission and Competent Authorities for Medical Devices (CAMD) organised their first multi-stakeholder implementation workshop, which EUCOPE attended and have kindly provided a summary of the meeting below.

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Published on 13. March 2017 in News EU